CAMSAP1 antibody (AA 1401-1500) (Biotin)

Catalog No. ABIN1700627

The Rabbit Polyclonal anti-CAMSAP1 antibody has been validated for WB, ELISA, IHC (p) and IHC (fro). It is suitable to detect CAMSAP1 in samples from Human.

Quick Overview for CAMSAP1 antibody (AA 1401-1500) (Biotin) (ABIN1700627)

Target: CAMSAP1 (Calmodulin Regulated Spectrin Associated Protein 1 (CAMSAP1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CAMSAP1 antibody is conjugated to Biotin

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Product Details anti-CAMSAP1 Antibody (Biotin)

Binding Specificity: AA 1401-1500

Predicted Reactivity: Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Chicken

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CAMSAP1

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C for 12 months.

Expiry Date: 12 months

Target Details for CAMSAP1

Target: CAMSAP1 (Calmodulin Regulated Spectrin Associated Protein 1 (CAMSAP1))

Alternative Name: CAMSAP1

Background:

Synonyms: calmodulin regulated spectrin-associated protein 1, Calmodulin-regulated spectrin-associated protein 1, CAMP1_HUMAN, camsap1, PRO2405.

Background: CAMSAP1L1 is a 1,489 amino acid protein that contains one calponin-homology domain and one CKK domain, which serves to bind microtubules. There are three isoforms of CAMSAP1L1 that are produced as a result of alternative splicing events. The gene encoding CAMSAP1L1 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1.

Gene ID: 157922